TWI701237B - 有機分子,特別是用於有機光電器件的有機分子 - Google Patents
有機分子,特別是用於有機光電器件的有機分子 Download PDFInfo
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- TWI701237B TWI701237B TW106128787A TW106128787A TWI701237B TW I701237 B TWI701237 B TW I701237B TW 106128787 A TW106128787 A TW 106128787A TW 106128787 A TW106128787 A TW 106128787A TW I701237 B TWI701237 B TW I701237B
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- 0 CCC1C*CC1 Chemical compound CCC1C*CC1 0.000 description 29
- FJNHUAOMROXELM-UHFFFAOYSA-N Cc(cc1)ccc1-c(cc1)cc(c2c3cccc2)c1[n]3-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n](c(ccc(-c2ccc(C)cc2)c2)c2c2c3)c2ccc3-c2cc(-c(cc3)cc4c3c3ccccc3[n]4-c(cc(cc3-[n]4c5cc(-c6ccc(C)c(-c(cc7)c(C)cc7-c(cc7c8c9ccc(-c%10cccc(C)c%10)c8)ccc7[n]9-c(cc(cc7-[n]8c(ccc(-c9cccc(C)c9)c9)c9c9c8ccc(-c8cc(C)ccc8)c9)-c8cc(C(F)(F)F)cc(C(F)(F)F)c8)c7C#N)c6)ccc5c5c4cccc5)-c4cc(C(F)(F)F)cc(C(F)(F)F)c4)c3C#N)ccc2C)c1C#N Chemical compound Cc(cc1)ccc1-c(cc1)cc(c2c3cccc2)c1[n]3-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n](c(ccc(-c2ccc(C)cc2)c2)c2c2c3)c2ccc3-c2cc(-c(cc3)cc4c3c3ccccc3[n]4-c(cc(cc3-[n]4c5cc(-c6ccc(C)c(-c(cc7)c(C)cc7-c(cc7c8c9ccc(-c%10cccc(C)c%10)c8)ccc7[n]9-c(cc(cc7-[n]8c(ccc(-c9cccc(C)c9)c9)c9c9c8ccc(-c8cc(C)ccc8)c9)-c8cc(C(F)(F)F)cc(C(F)(F)F)c8)c7C#N)c6)ccc5c5c4cccc5)-c4cc(C(F)(F)F)cc(C(F)(F)F)c4)c3C#N)ccc2C)c1C#N FJNHUAOMROXELM-UHFFFAOYSA-N 0.000 description 1
- PZHYKZURUZQTNN-UHFFFAOYSA-N Cc(cc1C)cc(C)c1-c(cc1)cc([n](c2c3)-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c(cc(cc6)-c7c(C)cc(C)cc7C)c6c(cc6)c5cc6-c5c(C)cc(C)cc5C)c4C#N)c1c2ccc3-c1c(C)cc(C)cc1C Chemical compound Cc(cc1C)cc(C)c1-c(cc1)cc([n](c2c3)-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c(cc(cc6)-c7c(C)cc(C)cc7C)c6c(cc6)c5cc6-c5c(C)cc(C)cc5C)c4C#N)c1c2ccc3-c1c(C)cc(C)cc1C PZHYKZURUZQTNN-UHFFFAOYSA-N 0.000 description 1
- JNOJXOOLKHQCGO-UHFFFAOYSA-N Cc(cc1C)cc(C)c1-c(cc1)cc(c2cc(-c3c(C)cc(C)cc3C)ccc22)c1[n]2-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n]2c(ccc(-c3c(C)cc(C)cc3C)c3)c3c3c2ccc(-c2c(C)cc(C)cc2C)c3)c1C#N Chemical compound Cc(cc1C)cc(C)c1-c(cc1)cc(c2cc(-c3c(C)cc(C)cc3C)ccc22)c1[n]2-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n]2c(ccc(-c3c(C)cc(C)cc3C)c3)c3c3c2ccc(-c2c(C)cc(C)cc2C)c3)c1C#N JNOJXOOLKHQCGO-UHFFFAOYSA-N 0.000 description 1
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- CJYIAKRXIIORQA-UHFFFAOYSA-N Cc(cccc1)c1-c(cc1)cc([n](c2c3)-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c(cc(cc6)-c7c(C)cccc7)c6c(cc6)c5cc6-c5ccccc5C)c4C#N)c1c2ccc3-c1c(C)cccc1 Chemical compound Cc(cccc1)c1-c(cc1)cc([n](c2c3)-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c(cc(cc6)-c7c(C)cccc7)c6c(cc6)c5cc6-c5ccccc5C)c4C#N)c1c2ccc3-c1c(C)cccc1 CJYIAKRXIIORQA-UHFFFAOYSA-N 0.000 description 1
- ABCDLASBLOMTOA-UHFFFAOYSA-N Cc1cc(-c(cc2)cc([n](c3c4)-c5cc(-c6cc(C(F)(F)F)cc(C(F)(F)F)c6)cc(-[n](c6c7)c8cc(-c9cc(C)ccc9)ccc8c6ccc7-c6cc(C)ccc6)c5C#N)c2c3ccc4-c2cccc(C)c2)ccc1 Chemical compound Cc1cc(-c(cc2)cc([n](c3c4)-c5cc(-c6cc(C(F)(F)F)cc(C(F)(F)F)c6)cc(-[n](c6c7)c8cc(-c9cc(C)ccc9)ccc8c6ccc7-c6cc(C)ccc6)c5C#N)c2c3ccc4-c2cccc(C)c2)ccc1 ABCDLASBLOMTOA-UHFFFAOYSA-N 0.000 description 1
- IORPOSRFVWMUCL-UHFFFAOYSA-N Cc1cc(-c(cc2-[n]3c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)ccc4c4c3cccc4)cc(-[n]3c(cc(cc4)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4c4c3cccc4)c2C#N)cc(C(F)(F)F)c1 Chemical compound Cc1cc(-c(cc2-[n]3c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)ccc4c4c3cccc4)cc(-[n]3c(cc(cc4)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4c4c3cccc4)c2C#N)cc(C(F)(F)F)c1 IORPOSRFVWMUCL-UHFFFAOYSA-N 0.000 description 1
- LBBJFVTXVSRNBW-UHFFFAOYSA-N Cc1cccc(-c(cc2)cc(c3c4cccc3)c2[n]4-c(cc(cc2-[n]3c(ccc(-c4cccc(C)c4)c4)c4c4c3cccc4)-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)c2C#N)c1 Chemical compound Cc1cccc(-c(cc2)cc(c3c4cccc3)c2[n]4-c(cc(cc2-[n]3c(ccc(-c4cccc(C)c4)c4)c4c4c3cccc4)-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)c2C#N)c1 LBBJFVTXVSRNBW-UHFFFAOYSA-N 0.000 description 1
- ZOGLONFSSQGACY-UHFFFAOYSA-N Cc1cccc(-c2ccc(c(cccc3)c3[n]3-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c6cc(-c7cccc(C)c7)ccc6c6c5cccc6)c4C#N)c3c2)c1 Chemical compound Cc1cccc(-c2ccc(c(cccc3)c3[n]3-c4cc(-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)cc(-[n]5c6cc(-c7cccc(C)c7)ccc6c6c5cccc6)c4C#N)c3c2)c1 ZOGLONFSSQGACY-UHFFFAOYSA-N 0.000 description 1
- WJQHWURILKGUNC-UHFFFAOYSA-N N#Cc(c(-[n](c(ccc(-c1c(C(F)(F)F)cc(C(F)(F)F)cc1)c1)c1c1c2)c1ccc2-c1ccc(C(F)(F)F)cc1C(F)(F)F)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c(ccc(-c2c(C(F)(F)F)cc(C(F)(F)F)cc2)c2)c2c2c1ccc(-c1c(C(F)(F)F)cc(C(F)(F)F)cc1)c2 Chemical compound N#Cc(c(-[n](c(ccc(-c1c(C(F)(F)F)cc(C(F)(F)F)cc1)c1)c1c1c2)c1ccc2-c1ccc(C(F)(F)F)cc1C(F)(F)F)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c(ccc(-c2c(C(F)(F)F)cc(C(F)(F)F)cc2)c2)c2c2c1ccc(-c1c(C(F)(F)F)cc(C(F)(F)F)cc1)c2 WJQHWURILKGUNC-UHFFFAOYSA-N 0.000 description 1
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- VCJUCSXMSWFGGW-UHFFFAOYSA-N N#Cc(c(-[n]1c(ccc(-c2ccc(C(F)(F)F)cc2C(F)(F)F)c2)c2c2c1cccc2)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c(ccc(-c2c(C(F)(F)F)cc(C(F)(F)F)cc2)c2)c2c2ccccc12 Chemical compound N#Cc(c(-[n]1c(ccc(-c2ccc(C(F)(F)F)cc2C(F)(F)F)c2)c2c2c1cccc2)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c(ccc(-c2c(C(F)(F)F)cc(C(F)(F)F)cc2)c2)c2c2ccccc12 VCJUCSXMSWFGGW-UHFFFAOYSA-N 0.000 description 1
- QQMJNTMWEXYTSC-UHFFFAOYSA-N N#Cc(c(-[n]1c2cc(-c3c(C(F)(F)F)cc(C(F)(F)F)cc3)ccc2c2ccccc12)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c2cc(-c3c(C(F)(F)F)cc(C(F)(F)F)cc3)ccc2c2c1cccc2 Chemical compound N#Cc(c(-[n]1c2cc(-c3c(C(F)(F)F)cc(C(F)(F)F)cc3)ccc2c2ccccc12)cc(-c1cc(C(F)(F)F)cc(C(F)(F)F)c1)c1)c1-[n]1c2cc(-c3c(C(F)(F)F)cc(C(F)(F)F)cc3)ccc2c2c1cccc2 QQMJNTMWEXYTSC-UHFFFAOYSA-N 0.000 description 1
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- TTZCFVSHWHOLLP-UHFFFAOYSA-N N#Cc1cc(-c(cc2)cc(c3c4ccc(-c5cccc(C#N)c5)c3)c2[n]4-c2cc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cc(-[n]3c(ccc(-c4cc(C#N)ccc4)c4)c4c4c3ccc(-c3cc(C#N)ccc3)c4)c2C#N)ccc1 Chemical compound N#Cc1cc(-c(cc2)cc(c3c4ccc(-c5cccc(C#N)c5)c3)c2[n]4-c2cc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cc(-[n]3c(ccc(-c4cc(C#N)ccc4)c4)c4c4c3ccc(-c3cc(C#N)ccc3)c4)c2C#N)ccc1 TTZCFVSHWHOLLP-UHFFFAOYSA-N 0.000 description 1
- YFCFMJCCEONGJT-UHFFFAOYSA-N N#Cc1cc(-c2ccc(c(ccc(-c3cccc(C#N)c3)c3)c3[n]3-c(cc(cc4-[n]5c(cc(cc6)-c7cc(C#N)ccc7)c6c(cc6)c5cc6-c5cc(C#N)ccc5)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4C#N)c3c2)ccc1 Chemical compound N#Cc1cc(-c2ccc(c(ccc(-c3cccc(C#N)c3)c3)c3[n]3-c(cc(cc4-[n]5c(cc(cc6)-c7cc(C#N)ccc7)c6c(cc6)c5cc6-c5cc(C#N)ccc5)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4C#N)c3c2)ccc1 YFCFMJCCEONGJT-UHFFFAOYSA-N 0.000 description 1
- OMZBCUWFQZMCLS-UHFFFAOYSA-N N#Cc1cccc(-c(cc2)cc(c3c4cccc3)c2[n]4-c2cc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cc(-[n](c(ccc(-c3cccc(C#N)c3)c3)c3c3c4)c3ccc4-c3cc(C#N)cc(-c(cc4)cc5c4c(cccc4)c4[n]5-c(cc(cc4-[n]5c(cc(cc6)-c7cc(C#N)ccc7)c6c6c5cccc6)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4C#N)c3)c2C#N)c1 Chemical compound N#Cc1cccc(-c(cc2)cc(c3c4cccc3)c2[n]4-c2cc(-c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cc(-[n](c(ccc(-c3cccc(C#N)c3)c3)c3c3c4)c3ccc4-c3cc(C#N)cc(-c(cc4)cc5c4c(cccc4)c4[n]5-c(cc(cc4-[n]5c(cc(cc6)-c7cc(C#N)ccc7)c6c6c5cccc6)-c5cc(C(F)(F)F)cc(C(F)(F)F)c5)c4C#N)c3)c2C#N)c1 OMZBCUWFQZMCLS-UHFFFAOYSA-N 0.000 description 1
- BTFVAGWXGHBRQA-UHFFFAOYSA-N N#Cc1ccccc1-c(cc1)cc(c2cc(-c3ccccc3C#N)ccc22)c1[n]2-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n]2c(ccc(-c(cccc3)c3C#N)c3)c3c3c2ccc(-c(cccc2)c2C#N)c3)c1C#N Chemical compound N#Cc1ccccc1-c(cc1)cc(c2cc(-c3ccccc3C#N)ccc22)c1[n]2-c1cc(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)cc(-[n]2c(ccc(-c(cccc3)c3C#N)c3)c3c3c2ccc(-c(cccc2)c2C#N)c3)c1C#N BTFVAGWXGHBRQA-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/86—Carbazoles; Hydrogenated carbazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/94—[b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
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Applications Claiming Priority (12)
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| DE102016115854.2 | 2016-08-25 | ||
| DE102016115854.2A DE102016115854B3 (de) | 2016-08-25 | 2016-08-25 | Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen |
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| US10971688B2 (en) * | 2016-10-25 | 2021-04-06 | Cynora Gmbh | Organic molecules for use in organic optoelectronic devices |
| EP3398945B1 (en) * | 2017-05-04 | 2022-11-02 | Samsung Display Co., Ltd. | Pyrimidinyl derivatives and their use in optoelectronic devices |
| DE102017109593B4 (de) | 2017-05-04 | 2018-12-13 | Cynora Gmbh | Organische Moleküle, insbesondere zur Verwendung in optoelektronischen Vorrichtungen |
| WO2018224421A1 (en) | 2017-06-06 | 2018-12-13 | Cynora Gmbh | Organic molecules, in particular for use in optoelectronic devices |
| CN110785407B (zh) * | 2017-06-22 | 2023-10-03 | 三星显示有限公司 | 有机分子,特别是用于光电装置的有机分子 |
| EP3645524B1 (en) * | 2017-06-28 | 2021-11-24 | cynora GmbH | Organic molecules, in particular for use in optoelectronic devices |
| DE102017114345B4 (de) * | 2017-06-28 | 2019-01-17 | Cynora Gmbh | Organische Moleküle, insbesondere zur Verwendung in organischen optoelektronischen Vorrichtungen |
| JP7165943B2 (ja) * | 2017-11-01 | 2022-11-07 | 東洋紡株式会社 | π電子共役単位とカルバゾール基を有する化合物 |
| WO2019166666A1 (en) * | 2018-03-02 | 2019-09-06 | Cynora Gmbh | Organic molecules for optoelectronic devices |
| EP3781559B1 (en) * | 2018-04-17 | 2025-01-22 | Samsung Display Co., Ltd. | Organic molecules for optoelectronic devices |
| KR102692561B1 (ko) * | 2018-06-26 | 2024-08-06 | 삼성전자주식회사 | 유기 발광 소자 |
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| US20230209847A1 (en) * | 2020-05-29 | 2023-06-29 | Kyulux, Inc. | Organic light emitting element |
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| EP2976329B1 (de) | 2013-03-22 | 2018-06-27 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| US20160126478A1 (en) * | 2013-05-09 | 2016-05-05 | Nitto Denko Corporation | Emissive compounds for light emitting devices |
| WO2015066354A1 (en) * | 2013-10-30 | 2015-05-07 | Nitto Denko Corporation | Light-emitting compounds for light-emitting devices |
| US20170244049A1 (en) * | 2014-05-14 | 2017-08-24 | President And Fellows Of Harvard College | Organic light-emitting diode materials |
| WO2016138077A1 (en) * | 2015-02-24 | 2016-09-01 | Nitto Denko Corporation | Gas sensor element |
| CN106966955A (zh) | 2017-04-21 | 2017-07-21 | 瑞声光电科技(常州)有限公司 | 联苯化合物及发光器件 |
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